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{2-[(Anthracene-9-carbonyl)-amino]-acetylamino}-acetic acid 11-[(Z)-3-(2,2-diphenyl-ethylcarbamoyl)-acryloylamino]-undecyl ester

Base Information Edit
  • Chemical Name:{2-[(Anthracene-9-carbonyl)-amino]-acetylamino}-acetic acid 11-[(Z)-3-(2,2-diphenyl-ethylcarbamoyl)-acryloylamino]-undecyl ester
  • CAS No.:792917-47-6
  • Molecular Formula:C48H54N4O6
  • Molecular Weight:782.98
  • Hs Code.:
  • Mol file:792917-47-6.mol
{2-[(Anthracene-9-carbonyl)-amino]-acetylamino}-acetic acid 11-[(Z)-3-(2,2-diphenyl-ethylcarbamoyl)-acryloylamino]-undecyl ester

Synonyms:{2-[(Anthracene-9-carbonyl)-amino]-acetylamino}-acetic acid 11-[(Z)-3-(2,2-diphenyl-ethylcarbamoyl)-acryloylamino]-undecyl ester

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Chemical Property of {2-[(Anthracene-9-carbonyl)-amino]-acetylamino}-acetic acid 11-[(Z)-3-(2,2-diphenyl-ethylcarbamoyl)-acryloylamino]-undecyl ester Edit
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Technology Process of {2-[(Anthracene-9-carbonyl)-amino]-acetylamino}-acetic acid 11-[(Z)-3-(2,2-diphenyl-ethylcarbamoyl)-acryloylamino]-undecyl ester

There total 6 articles about {2-[(Anthracene-9-carbonyl)-amino]-acetylamino}-acetic acid 11-[(Z)-3-(2,2-diphenyl-ethylcarbamoyl)-acryloylamino]-undecyl ester which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
Multi-step reaction with 6 steps
1: 98 percent / dimethylformamide / 2 h / 80 °C
2: hydrazine hydrate / ethanol / 0.5 h / Heating
3: 100 percent / NaOH / methanol
4: 60 percent / 4-(dimethylamino)pyridine; 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride / CHCl3 / 6 h / 20 °C
5: trifluoroacetic acid / CH2Cl2
6: 55 percent / 4-(dimethylaminp)pyridine; 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride / CH2Cl2; dimethylformamide / 20 °C
With dmap; sodium hydroxide; hydrazine hydrate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; trifluoroacetic acid; In methanol; ethanol; dichloromethane; chloroform; N,N-dimethyl-formamide;
DOI:10.1021/ja0484193
Guidance literature:
Multi-step reaction with 4 steps
1: 100 percent / NaOH / methanol
2: 60 percent / 4-(dimethylamino)pyridine; 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride / CHCl3 / 6 h / 20 °C
3: trifluoroacetic acid / CH2Cl2
4: 55 percent / 4-(dimethylaminp)pyridine; 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride / CH2Cl2; dimethylformamide / 20 °C
With dmap; sodium hydroxide; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; trifluoroacetic acid; In methanol; dichloromethane; chloroform; N,N-dimethyl-formamide;
DOI:10.1021/ja0484193
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